(Q43598098)

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Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.

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6 February 2020

Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22745357%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

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Claudio Rapezzi

1

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6 February 2020

Giovanni Palladini

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6 February 2020

Giampaolo Merlini

17

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6 February 2020

Candida Cristina Quarta

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6 February 2020

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6 February 2020

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6 February 2020

Massimiliano Lorenzini

8

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6 February 2020

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6 February 2020

Francesco Cappelli

11

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6 February 2020

Stefano Perlini

18

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6 February 2020

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Federico Perfetto

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6 February 2020

Simone Longhi

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6 February 2020

Fabrizio Salvi

6

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6 February 2020

Francesco Grigioni

9

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6 February 2020

Paola Rimessi

13

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6 February 2020

Alessandra Ferlini

14

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6 February 2020

Giorgio Arpesella

15

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6 February 2020

Antonio Daniele Pinna

16

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6 February 2020

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28 June 2012

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6 February 2020

European Heart Journal

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6 February 2020

34

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6 February 2020

7

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6 February 2020

520-528

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6 February 2020

Transthyretin-related familial amyloidotic polyneuropathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Hereditary transthyretin amyloidosis from a Scandinavian perspective.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Phenotypic expression of familial amyloid polyneuropathy in Brazil.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Transthyretin-related amyloidoses and the heart: a clinical overview

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

A Danish kindred with familial amyloid cardiomyopathy revisited: Identification of a mutant transthyretinmethionine111 variant in serum from patients and carriers

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Amyloid heart disease

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Infiltrative cardiovascular diseases: cardiomyopathies that look alike

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18-22 April 2004.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

The molecular biology and clinical features of amyloid neuropathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

ACC/AHA/ASE 2003 Guideline Update for the Clinical Application of Echocardiography: Summary Article: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (ACC/AHA/ASE Committee to Update the 1997

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Late occurrence of fatal aortitis: a complication of Aspergillus endocarditis following coronary artery bypass graft surgery.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Prevalence of carpal tunnel syndrome in a general population

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

The biological and chemical basis for tissue-selective amyloid disease

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Why are some amyloidoses systemic? Does hepatic "chaperoning at a distance" prevent cardiac deposition in a transgenic model of human senile systemic (transthyretin) amyloidosis?

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Gender-related risk of myocardial involvement in systemic amyloidosis.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Pressure-volume relationships in patients with transthyretin (ATTR) cardiac amyloidosis secondary to V122I mutations and wild-type transthyretin: Transthyretin Cardiac Amyloid Study (TRACS).

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Heart transplantation for homozygous familial transthyretin (TTR) V122I cardiac amyloidosis.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Orally administered diflunisal stabilizes transthyretin against dissociation required for amyloidogenesis

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

Cardiac amyloidosis in African Americans: Comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosis

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHS123

21 January 2018

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